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4''-O-(2-(4-methoxyphenyl)-1H-benzimidazole-5-carbonyl)hydrazinecarbonylclarithromycin

Base Information
  • Chemical Name:4''-O-(2-(4-methoxyphenyl)-1H-benzimidazole-5-carbonyl)hydrazinecarbonylclarithromycin
  • CAS No.:1259500-80-5
  • Molecular Formula:C54H81N5O16
  • Molecular Weight:1056.26
  • Hs Code.:
4''-O-(2-(4-methoxyphenyl)-1H-benzimidazole-5-carbonyl)hydrazinecarbonylclarithromycin

Synonyms:4''-O-(2-(4-methoxyphenyl)-1H-benzimidazole-5-carbonyl)hydrazinecarbonylclarithromycin

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Chemical Property of 4''-O-(2-(4-methoxyphenyl)-1H-benzimidazole-5-carbonyl)hydrazinecarbonylclarithromycin
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Technology Process of 4''-O-(2-(4-methoxyphenyl)-1H-benzimidazole-5-carbonyl)hydrazinecarbonylclarithromycin

There total 7 articles about 4''-O-(2-(4-methoxyphenyl)-1H-benzimidazole-5-carbonyl)hydrazinecarbonylclarithromycin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1.1: hydrazine hydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 7 h / 20 °C
2.1: tetrahydrofuran / 20 °C
2.2: Saturated solution
3.1: methanol / 8 h / 75 °C
With methanol; hydrazine hydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.04.004
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium metabisulfite / ethanol; water / 20 °C
1.2: 130 °C
2.1: thionyl chloride / 8 h / Reflux
3.1: tetrahydrofuran / 20 °C
3.2: Saturated solution
4.1: methanol / 8 h / 75 °C
With methanol; sodium metabisulfite; thionyl chloride; In tetrahydrofuran; ethanol; water;
DOI:10.1016/j.ejmech.2011.04.004
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